Evidence map›Paper›PMID 42852223›Full record

ArticleACS omega2026

Fast-Dissolving and Highly Soluble Dasatinib Multicomponent Crystals Efficiently Inhibit Leukemia Cell Viability.

Luan F Diniz, Luiz C G Diógenes, Paulo S Carvalho, Ezequiel A D Junior, Alexia D Nascimento, Maria E Cortés, Rubén Dario Sinisterra, Renata Diniz, Christian Fernandes

Abstract read
In one paragraph

Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Luan F DinizDepartamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.
Luiz C G DiógenesDepartamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.
Paulo S CarvalhoInstituto de Física, Universidade Federal do Mato Grosso do Sul, 79074-460 Campo Grande, MS, Brazil.ORCID https://orcid.org/0000-0002-5551-9155
Ezequiel A D JuniorDepartamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.
Alexia D NascimentoDepartamento de Odontologia Restauradora, Faculdade de Odontologia, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0001-6358-4806
Maria E CortésDepartamento de Odontologia Restauradora, Faculdade de Odontologia, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0002-0560-8491
Rubén Dario SinisterraInovação Tecnológica, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0001-7656-1849
Renata DinizDepartamento de Química, Instituto de Ciências Exatas (ICEx), Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0001-9042-9094
Christian FernandesDepartamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0002-3905-3674

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dasatinib (DAS) is a biopharmaceutical classification system (BCS) class II drug that is used orally to treat chronic myelogenous leukemia. However, its very low and pH-dependent aqueous solubility severely limits its oral bioavailability. To address this biopharmaceutical limitation, we designed more soluble multicomponent crystalline forms (MCCs) of DAS. Two novel salt solvate forms were successfully obtained via solvent evaporation through reactions with maleic and fumaric acids. A comprehensive solid-state evaluation of these salt solvate forms was conducted by using X-ray diffraction (SCXRD, PXRD), spectroscopy (FT-IR and

Identifiers

PMID42852223
PMCPMC13647392

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.